HGVS | Genome Assembly |
---|---|
NC_000010.11:g.55089127_55089128delinsAT , CM000672.2:g.55089127_55089128delinsAT | GRCh38 |
NC_000010.10:g.56848887_56848888delinsAT , CM000672.1:g.56848887_56848888delinsAT | GRCh37 |
NC_000010.9:g.56518893_56518894delinsAT | NCBI36 |
NG_009191.3:g.545055_545056delinsAT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000458638.1:c.-80+77448_-80+77449delinsAT | ENSP00000394465.1:n.-80+77448_-80+77449de... | |
ENST00000613346.4:c.-80+77448_-80+77449delinsAT | ENSP00000481211.1:n.-80+77448_-80+77449de... | |
NM_001354404.1:c.-80+77448_-80+77449delinsAT | NP_001341333.1:n.-80+77448_-80+77449delin... | |
XM_017016573.2:c.-157+77448_-157+77449delinsAT | XP_016872062.1:n.-157+77448_-157+77449del... | |
NM_001354404.2:c.-80+77448_-80+77449delinsAT | NP_001341333.1:n.-80+77448_-80+77449delin... |